Variant report

Variant	rs530051580
Chromosome Location	chr1:180199399-180199400
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:180199260-180199676	K562	blood:	n/a	n/a
2	ZNF263	chr1:180199360-180201641	HEK293-T-REx	kidney:	n/a	n/a
3	CHD2	chr1:180199170-180199684	H1-hESC	embryonic stem cell:	n/a	chr1:180199487-180199497
4	MAX	chr1:180198568-180199536	MCF-7	breast:	n/a	chr1:180199482-180199492
5	CREB1	chr1:180198879-180199615	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr1:180199143-180199557	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTBP2	chr1:180199283-180201455	H1-hESC	embryonic stem cell:	n/a	n/a
8	HDAC2	chr1:180199144-180199462	K562	blood:	n/a	n/a
9	MAX	chr1:180197799-180199538	ECC-1	luminal epithelium:	n/a	chr1:180199482-180199492
10	POLR2A	chr1:180199264-180200017	H1-neurons	neurons:	n/a	n/a
11	EGR1	chr1:180198877-180199488	K562	blood:	n/a	chr1:180199316-180199326
12	CHD2	chr1:180199394-180199563	K562	blood:	n/a	chr1:180199487-180199497
13	TCF7L2	chr1:180199377-180199739	Hela-S3	cervix:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465
14	TCF12	chr1:180198930-180199724	ECC-1	luminal epithelium:	n/a	n/a
15	MYC	chr1:180198627-180199753	NB4	blood:	n/a	chr1:180199482-180199492
16	TCF12	chr1:180198662-180199804	ECC-1	luminal epithelium:	n/a	n/a
17	ZNF143	chr1:180199386-180199510	K562	blood:	n/a	n/a
18	UBTF	chr1:180199299-180199612	K562	blood:	n/a	n/a
19	ZBTB7A	chr1:180198135-180200333	ECC-1	luminal epithelium:	n/a	n/a
20	ZBTB7A	chr1:180199124-180199567	K562	blood:	n/a	n/a
21	ELF1	chr1:180199229-180199872	GM12878	blood:	n/a	n/a
22	CREB1	chr1:180199137-180199448	A549	lung:	n/a	n/a
23	TCF7L2	chr1:180199315-180201430	Hela-S3	cervix:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465
24	SIN3A	chr1:180198105-180201535	H1-hESC	embryonic stem cell:	n/a	chr1:180199800-180199811 chr1:180201367-180201377 chr1:180200185-180200198 chr1:180198586-180198597 chr1:180198584-180198597
25	TCF7L2	chr1:180199154-180199812	HCT-116	colon:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465
26	MAX	chr1:180197655-180199566	H1-hESC	embryonic stem cell:	n/a	chr1:180199482-180199492
27	POLR2A	chr1:180198562-180199636	HEK293	kidney:	n/a	n/a
28	EGR1	chr1:180198795-180199473	MCF-7	breast:	n/a	chr1:180199316-180199326
29	POLR2A	chr1:180198687-180199573	MCF-7	breast:	n/a	n/a
30	CHD2	chr1:180199001-180200978	Hela-S3	cervix:	n/a	chr1:180199487-180199497 chr1:180199805-180199815
31	MAX	chr1:180197976-180199478	K562	blood:	n/a	n/a
32	NFIC	chr1:180199177-180199678	ECC-1	luminal epithelium:	n/a	n/a
33	TCF7L2	chr1:180199370-180199671	MCF-7	breast:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465
34	RCOR1	chr1:180198591-180199493	K562	blood:	n/a	n/a
35	SP1	chr1:180199145-180199725	A549	lung:	n/a	chr1:180199488-180199497 chr1:180199487-180199499 chr1:180199487-180199499 chr1:180199484-180199498
36	TCF7L2	chr1:180199355-180201054	PANC-1	pancreas:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465
37	MAX	chr1:180197703-180201188	A549	lung:	n/a	chr1:180199482-180199492 chr1:180200203-180200213 chr1:180200952-180200961
38	MAX	chr1:180199153-180199416	K562	blood:	n/a	n/a
39	TBP	chr1:180198651-180199458	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAX	chr1:180197791-180199659	A549	lung:	n/a	chr1:180199482-180199492
41	E2F6	chr1:180199168-180199420	K562	blood:	n/a	chr1:180199215-180199225 chr1:180199214-180199223
42	SMC3	chr1:180199324-180199845	Hela-S3	cervix:	n/a	n/a
43	FOXP2	chr1:180198403-180199555	PFSK-1	brain:	n/a	n/a
44	HDAC2	chr1:180199158-180199486	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr1:180198701-180199557	NB4	blood:	n/a	chr1:180199482-180199492
46	MAZ	chr1:180198645-180199534	K562	blood:	n/a	chr1:180199482-180199492
47	MAX	chr1:180197826-180199410	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAZ	chr1:180198851-180199949	Hela-S3	cervix:	n/a	chr1:180199482-180199492
49	ZBTB7A	chr1:180198771-180200521	ECC-1	luminal epithelium:	n/a	n/a
50	TCF7L2	chr1:180199259-180200400	HEK293	kidney:	n/a	chr1:180199449-180199463 chr1:180199451-180199461 chr1:180199453-180199462 chr1:180199449-180199465 chr1:180199450-180199464 chr1:180199452-180199461 chr1:180199449-180199465

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180199374-180199424	PANC-1	pancreas:	n/a
2	chr1:180199374-180199424	LNCaP	prostate:	n/a
3	chr1:180199374-180199424	K562	blood:	n/a
4	chr1:180199374-180199424	NHDF-neo	bronchial:	n/a
5	chr1:180199374-180199424	HIPEpiC	eye:	n/a
6	chr1:180199374-180199424	ProgFib	skin:	n/a
7	chr1:180199374-180199424	Hela-S3	cervix:	n/a
8	chr1:180199374-180199424	HUVEC	blood vessel:	n/a
9	chr1:180199374-180199424	GM06990	blood:	n/a
10	chr1:180199374-180199424	BJ	skin:	n/a
11	chr1:180199374-180199424	PFSK-1	brain:	n/a
12	chr1:180199374-180199424	MCF10A-Er-Src	breast:	n/a
13	chr1:180199374-180199424	HL-60	blood:	n/a
14	chr1:180199374-180199424	AG10803	skin:	n/a
15	chr1:180199374-180199424	SKMC	muscle:	n/a
16	chr1:180199374-180199424	AG09309	skin:	n/a
17	chr1:180199374-180199424	MCF-7	breast:	n/a
18	chr1:180199374-180199424	SK-N-MC	brain:	n/a
19	chr1:180199374-180199424	HEK293	kidney:	embryo
20	chr1:180199374-180199424	AG04449	skin:	fetal
21	chr1:180199374-180199424	AoSMC	blood vessel:	n/a
22	chr1:180199374-180199424	HCF	heart:	n/a
23	chr1:180199374-180199424	BE2_C	brain:	n/a
24	chr1:180199374-180199424	ECC-1	luminal epithelium:	n/a
25	chr1:180199374-180199424	Jurkat	blood:	n/a
26	chr1:180199374-180199424	A549	lung:	n/a
27	chr1:180199374-180199424	T-47D	breast:	n/a
28	chr1:180199374-180199424	SAEC	small airway:	n/a
29	chr1:180199374-180199424	SK-N-SH_RA	brain:	n/a
30	chr1:180199374-180199424	HepG2	liver:	n/a
31	chr1:180199374-180199424	HEEpiC	esophagus:	n/a
32	chr1:180199374-180199424	HCT-116	colon:	n/a
33	chr1:180199374-180199424	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:180199374-180199424	AG09319	gingival:	n/a
35	chr1:180199374-180199424	GM12878	blood:	n/a
36	chr1:180199374-180199424	GM19239	blood:	n/a
37	chr1:180199374-180199424	NB4	blood:	n/a
38	chr1:180199374-180199424	HAEpiC	amniotic membrane:	n/a
39	chr1:180199374-180199424	NHBE	bronchial:	n/a
40	chr1:180199374-180199424	HCPEpiC	choroid plexus:	n/a
41	chr1:180199374-180199424	IMR90	lung:	fetal
42	chr1:180199374-180199424	SK-N-SH	brain:	n/a
43	chr1:180199374-180199424	GM12892	blood:	n/a
44	chr1:180199374-180199424	HMEC	breast:	n/a
45	chr1:180199374-180199424	U87	brain:	n/a
46	chr1:180199374-180199424	HCM	heart:	n/a
47	chr1:180199374-180199424	NT2-D1	testis:	n/a
48	chr1:180199374-180199424	RPTEC	kidney:	n/a
49	chr1:180199374-180199424	NH-A	brain:	n/a
50	chr1:180199374-180199424	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180197757..180200322-chr1:180217302..180220148,2	K562	blood:
2	chr1:180123935..180126561-chr1:180199070..180201304,3	MCF-7	breast:
3	chr1:180197528..180200245-chr1:180468948..180472883,3	MCF-7	breast:
4	chr1:180049598..180051873-chr1:180198863..180200788,2	MCF-7	breast:

Variant related genes	Relation type
LHX4	TF binding region
LHX4	CpG island
ENSG00000135837	Chromatin interaction
ENSG00000121454	Chromatin interaction
ENSG00000116260	Chromatin interaction
ENSG00000135847	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429936	chr1:179790343-180214343	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1003739	chr1:180027760-180483292	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv535217	chr1:180027760-180483292	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv1012558	chr1:180027960-180217613	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv535218	chr1:180027960-180217613	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv497930	chr1:180031321-180220723	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv533073	chr1:180031328-180217612	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv916937	chr1:180031328-180220685	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv1007590	chr1:180121480-180236452	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
10	nsv999104	chr1:180121480-180242659	Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1002133	chr1:180127036-180230081	Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv1011134	chr1:180127616-180201104	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv999182	chr1:180127616-180236452	Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv1005512	chr1:180127616-180242659	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv832004	chr1:180128502-180335540	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
16	nsv1012816	chr1:180132688-180201104	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
17	nsv1012145	chr1:180132688-180236452	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv466239	chr1:180145978-180268476	Bivalent Enhancer ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
19	nsv548345	chr1:180145978-180268476	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
20	nsv1005793	chr1:180150400-180205202	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
21	nsv1005073	chr1:180152550-180250783	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
22	nsv535219	chr1:180152550-180250783	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
23	nsv1001477	chr1:180172903-180298287	Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv535220	chr1:180172903-180298287	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv498075	chr1:180179441-180278544	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
26	nsv872575	chr1:180186713-180238243	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
27	esv3361812	chr1:180197754-180200702	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
28	esv14202	chr1:180198652-180200893	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180197400-180201000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr1:180197600-180201000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
3	chr1:180197800-180201000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr1:180197800-180201000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
5	chr1:180197800-180201000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr1:180197800-180201200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr1:180198000-180200600	Bivalent/Poised TSS	NHEK	skin
8	chr1:180198000-180201000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
9	chr1:180198200-180199600	Bivalent/Poised TSS	Fetal Brain Female	brain
10	chr1:180198200-180199600	Bivalent/Poised TSS	Osteobl	bone
11	chr1:180198200-180200000	Flanking Bivalent TSS/Enh	Thymus	Thymus
12	chr1:180198200-180201000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
13	chr1:180198400-180199400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:180198400-180199400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
15	chr1:180198400-180199400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:180198400-180199600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:180198400-180199600	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
18	chr1:180198400-180199600	Bivalent/Poised TSS	Brain Substantia Nigra	brain
19	chr1:180198400-180199600	Active TSS	K562	blood
20	chr1:180198400-180199800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:180198400-180200000	Active TSS	H9 Cell Line	embryonic stem cell
22	chr1:180198400-180200000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:180198400-180200000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
24	chr1:180198400-180200000	Active TSS	Hela-S3	cervix
25	chr1:180198400-180200400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
26	chr1:180198400-180200400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:180198400-180200400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:180198400-180200800	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr1:180198400-180200800	Active TSS	Aorta	Aorta
30	chr1:180198400-180200800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
31	chr1:180198400-180201000	Bivalent/Poised TSS	NHDF-Ad	bronchial
32	chr1:180198400-180201200	Active TSS	A549	lung
33	chr1:180198400-180201200	Active TSS	HSMMtube	muscle
34	chr1:180198600-180199400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:180198600-180199400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
36	chr1:180198600-180199400	Bivalent/Poised TSS	Fetal Intestine Small	intestine
37	chr1:180198600-180199400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
38	chr1:180198600-180199400	Bivalent/Poised TSS	Fetal Stomach	stomach
39	chr1:180198600-180199400	Active TSS	HSMM	muscle
40	chr1:180198600-180199600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:180198600-180199600	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:180198600-180199600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr1:180198600-180199600	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr1:180198600-180199600	Bivalent/Poised TSS	Left Ventricle	heart
45	chr1:180198600-180199800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr1:180198600-180199800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
47	chr1:180198600-180200800	Bivalent/Poised TSS	HepG2	liver
48	chr1:180198800-180199400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr1:180198800-180199400	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:180198800-180199400	Bivalent/Poised TSS	Primary monocytes fromperipheralblood	blood

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