Variant report

Variant	esv3337951
Chromosome Location	chr12:29288734-29303032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:302)
CpG islands
(count:610)
Chromatin interactive
region (count:5)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:29299199-29299376	K562	blood:	n/a	n/a
2	ATF2	chr12:29301888-29302308	GM12878	blood:	n/a	n/a
3	BACH1	chr12:29301402-29302837	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr12:29301107-29301264	A549	lung:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
5	BHLHE40	chr12:29301015-29301680	K562	blood:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
6	BHLHE40	chr12:29301082-29301377	GM12878	blood:	n/a	chr12:29301191-29301200 chr12:29301190-29301199 chr12:29301190-29301199
7	BHLHE40	chr12:29301956-29302429	K562	blood:	n/a	n/a
8	CCNT2	chr12:29301916-29302627	K562	blood:	n/a	chr12:29302353-29302362 chr12:29301930-29301939
9	CHD1	chr12:29302110-29302416	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr12:29301105-29301850	H1-hESC	embryonic stem cell:	n/a	chr12:29301793-29301800
11	CHD2	chr12:29298445-29298584	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr12:29301319-29302428	H1-hESC	embryonic stem cell:	n/a	chr12:29302083-29302093 chr12:29301793-29301800
13	CHD2	chr12:29301910-29302045	GM12878	blood:	n/a	n/a
14	CREB1	chr12:29302395-29303101	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr12:29301919-29303217	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr12:29301480-29301550	GM19238	blood:	n/a	n/a
17	CTCF	chr12:29301620-29301770	GM12873	blood:	n/a	n/a
18	CTCF	chr12:29301787-29301834	GM12878	blood:	n/a	n/a
19	CTCF	chr12:29301820-29301970	RPTEC	kidney:	n/a	n/a
20	CTCF	chr12:29301786-29301801	Gliobla	brain:	n/a	n/a
21	CTCF	chr12:29301700-29301850	HRE	kidney:	n/a	n/a
22	CTCF	chr12:29302500-29302650	Caco-2	colon:	n/a	chr12:29302536-29302549
23	CTCF	chr12:29301760-29301910	GM12871	blood:	n/a	n/a
24	CTCF	chr12:29301780-29301930	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr12:29301680-29301830	GM06990	blood:	n/a	n/a
26	CTCF	chr12:29301570-29301609	GM12891	blood:	n/a	n/a
27	CTCF	chr12:29301740-29301890	AG09319	gingival:	n/a	n/a
28	CTCF	chr12:29301781-29301785	Gliobla	brain:	n/a	n/a
29	CTCF	chr12:29301966-29302047	GM19238	blood:	n/a	n/a
30	CTCF	chr12:29301708-29301849	GM19240	blood:	n/a	n/a
31	CTCF	chr12:29301736-29301934	GM12878	blood:	n/a	n/a
32	CTCF	chr12:29301740-29301890	GM12874	blood:	n/a	n/a
33	CTCF	chr12:29302200-29302350	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr12:29301774-29301820	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr12:29301480-29301630	GM12865	blood:	n/a	n/a
36	CTCF	chr12:29301760-29301910	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr12:29301698-29301836	GM12891	blood:	n/a	n/a
38	CTCF	chr12:29301900-29302050	GM12864	blood:	n/a	n/a
39	CTCF	chr12:29301720-29301870	NB4	blood:	n/a	n/a
40	CTCF	chr12:29301440-29301590	GM12866	blood:	n/a	n/a
41	CTCF	chr12:29301760-29301910	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr12:29301780-29301930	AG09319	gingival:	n/a	n/a
43	CTCF	chr12:29301480-29301630	GM12874	blood:	n/a	n/a
44	CTCF	chr12:29301900-29302050	BJ	skin:	n/a	n/a
45	CTCF	chr12:29289375-29289424	Lung_OC	lung:	n/a	n/a
46	CTCF	chr12:29301673-29301889	GM19238	blood:	n/a	n/a
47	CTCF	chr12:29301800-29301950	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr12:29301667-29301670	GM19238	blood:	n/a	n/a
49	CTCF	chr12:29301660-29301810	BE2_C	brain:	n/a	n/a
50	CTCF	chr12:29301720-29301870	HCPEpiC	choroid plexus:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:29302515-29302565	IMR90	lung:	fetal
2	chr12:29302714-29302764	HCF	heart:	n/a
3	chr12:29302714-29302764	ProgFib	skin:	n/a
4	chr12:29301525-29301575	SK-N-MC	brain:	n/a
5	chr12:29302179-29302229	GM12878	blood:	n/a
6	chr12:29302016-29302066	Hela-S3	cervix:	n/a
7	chr12:29301719-29301769	HUVEC	blood vessel:	n/a
8	chr12:29302035-29302085	AG09309	skin:	n/a
9	chr12:29302714-29302764	K562	blood:	n/a
10	chr12:29302231-29302281	PrEC	prostate:	n/a
11	chr12:29302016-29302066	HUVEC	blood vessel:	n/a
12	chr12:29302231-29302281	NHBE	bronchial:	n/a
13	chr12:29302231-29302281	U87	brain:	n/a
14	chr12:29302279-29302329	SKMC	muscle:	n/a
15	chr12:29302016-29302066	HCF	heart:	n/a
16	chr12:29302279-29302329	SK-N-MC	brain:	n/a
17	chr12:29302714-29302764	AG04450	lung:	fetal
18	chr12:29302179-29302229	Caco-2	colon:	n/a
19	chr12:29302231-29302281	GM06990	blood:	n/a
20	chr12:29302714-29302764	AG04449	skin:	fetal
21	chr12:29302714-29302764	AG09319	gingival:	n/a
22	chr12:29299659-29299709	SK-N-SH	brain:	n/a
23	chr12:29301525-29301575	AG04449	skin:	fetal
24	chr12:29302515-29302565	AG09309	skin:	n/a
25	chr12:29302515-29302565	NT2-D1	testis:	n/a
26	chr12:29302714-29302764	HL-60	blood:	n/a
27	chr12:29302231-29302281	HRCEpiC	kidney:	n/a
28	chr12:29302279-29302329	ProgFib	skin:	n/a
29	chr12:29301525-29301575	CMK	blood:	n/a
30	chr12:29302016-29302066	GM06990	blood:	n/a
31	chr12:29302515-29302565	PrEC	prostate:	n/a
32	chr12:29302714-29302764	NHDF-neo	bronchial:	n/a
33	chr12:29302231-29302281	CMK	blood:	n/a
34	chr12:29302035-29302085	H1-hESC	embryonic stem cell:	embryo
35	chr12:29302515-29302565	A549	lung:	n/a
36	chr12:29302016-29302066	AG09309	skin:	n/a
37	chr12:29302231-29302281	HNPCEpiC	eye:	n/a
38	chr12:29302515-29302565	SK-N-SH_RA	brain:	n/a
39	chr12:29302016-29302066	HepG2	liver:	n/a
40	chr12:29302515-29302565	NB4	blood:	n/a
41	chr12:29299659-29299709	SK-N-SH_RA	brain:	n/a
42	chr12:29302231-29302281	AG09319	gingival:	n/a
43	chr12:29302515-29302565	H1-hESC	embryonic stem cell:	embryo
44	chr12:29301525-29301575	H1-hESC	embryonic stem cell:	embryo
45	chr12:29302279-29302329	HCPEpiC	choroid plexus:	n/a
46	chr12:29302035-29302085	HCT-116	colon:	n/a
47	chr12:29301525-29301575	Hepatocyte	liver:	n/a
48	chr12:29301525-29301575	K562	blood:	n/a
49	chr12:29302016-29302066	U87	brain:	n/a
50	chr12:29302016-29302066	HCPEpiC	choroid plexus:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:88070898..88071694-chr12:29302232..29303122,2	NB4	blood:
2	chr12:29301948..29302516-chr6:28806299..28806949,2	NB4	blood:
3	chr12:29301993..29302856-chr5:180670405..180671354,2	NB4	blood:
4	chr12:29302116..29302733-chr13:52025571..52026304,2	NB4	blood:
5	chr12:29301993..29302516-chr6:31802207..31802861,2	NB4	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-677C1.2.1-3	chr12:29302253-29302340	NONHSAT027484
2	lnc-ERGIC2-4	chr12:29301115-29301212	XLOC_010037
3	lnc-ERGIC2-3	chr12:29296129-29296581	ENSG00000257258
4	lnc-ERGIC2-4	chr12:29294264-29295242	XLOC_010037
5	lnc-ERGIC2-3	chr12:29301469-29301608	ENSG00000257258
6	lnc-RP11-677C1.2.1-3	chr12:29302143-29302340	NONHSAT027482

No data

Variant related genes	Relation type
ENSG00000257258	TF binding region
FAR2	TF binding region
ENSG00000257258	CpG island
FAR2	CpG island
ENSG00000102786	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000225173	chromatin interactions
ENSG00000204628	chromatin interactions
ENSG00000109861	chromatin interactions

Extended variants
information (count: 242 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:242 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540162496	chr12:29294289-29294290	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs189275709	chr12:29294355-29294356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs145037877	chr12:29294367-29294368	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs534361708	chr12:29294401-29294402	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs555172580	chr12:29294407-29294408	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs573447909	chr12:29294420-29294421	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs543888604	chr12:29294450-29294451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs369151443	chr12:29294461-29294462	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs78951741	chr12:29294547-29294548	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs544991345	chr12:29294586-29294587	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs560357011	chr12:29294738-29294739	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs527500009	chr12:29294757-29294758	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs181065510	chr12:29294782-29294783	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs186412553	chr12:29294798-29294799	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs552940765	chr12:29294810-29294811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs59113616	chr12:29294824-29294825	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376759120	chr12:29294838-29294839	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs551070462	chr12:29294912-29294913	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs562890051	chr12:29294923-29294924	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs533323251	chr12:29294941-29294942	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs191145177	chr12:29294958-29294959	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs181983912	chr12:29294975-29294976	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs147553253	chr12:29294997-29294998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs73273123	chr12:29295015-29295016	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573060110	chr12:29295025-29295026	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs201907135	chr12:29295032-29295033	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs567498412	chr12:29295053-29295054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs142378982	chr12:29295056-29295057	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs377030718	chr12:29295061-29295062	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs537571884	chr12:29295089-29295090	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs147058310	chr12:29295099-29295100	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs555807417	chr12:29295210-29295211	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs76839220	chr12:29295232-29295233	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs143492312	chr12:29295238-29295239	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs369451653	chr12:29295239-29295240	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs547835361	chr12:29296155-29296156	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs148770229	chr12:29296243-29296244	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs569346742	chr12:29296289-29296290	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs57418167	chr12:29296307-29296308	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs191608541	chr12:29296335-29296336	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs576311312	chr12:29296345-29296346	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs2117997	chr12:29296361-29296362	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs562986050	chr12:29296362-29296363	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs183065990	chr12:29296382-29296383	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs78205332	chr12:29296385-29296386	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs12320204	chr12:29296395-29296396	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545155813	chr12:29296402-29296403	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs61083639	chr12:29296404-29296405	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs527651570	chr12:29296423-29296424	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs118069201	chr12:29296425-29296426	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29298200-29299400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr12:29298400-29298600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:29298400-29298600	Enhancers	Fetal Muscle Trunk	muscle
4	chr12:29298400-29298800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:29298400-29299000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:29298400-29299600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr12:29298400-29299600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr12:29298600-29299400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr12:29298600-29300600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr12:29298600-29301000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr12:29298800-29299600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:29298800-29300000	Enhancers	Primary hematopoietic stem cells	blood
13	chr12:29299000-29299200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr12:29299000-29299600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:29299000-29300600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:29299000-29301200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:29299200-29299800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr12:29299200-29300800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr12:29299400-29300400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr12:29299400-29300600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr12:29299600-29300200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:29299600-29300600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:29299600-29301000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr12:29299600-29301200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:29299800-29300200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr12:29300000-29300400	Weak transcription	Primary hematopoietic stem cells	blood
27	chr12:29300200-29300600	Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr12:29300200-29301000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:29300200-29301600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:29300400-29300600	Enhancers	Primary hematopoietic stem cells	blood
31	chr12:29300400-29300600	Enhancers	NHDF-Ad	bronchial
32	chr12:29300400-29301000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr12:29300600-29300800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr12:29300600-29300800	Flanking Active TSS	NHDF-Ad	bronchial
35	chr12:29300600-29301000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr12:29300600-29301000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:29300600-29301000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr12:29300600-29301000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:29300600-29301000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr12:29300600-29301000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:29300600-29301000	Enhancers	Fetal Brain Female	brain
42	chr12:29300600-29301000	Enhancers	Dnd41	blood
43	chr12:29300600-29301000	Enhancers	HMEC	breast
44	chr12:29300600-29301000	Enhancers	HUVEC	blood vessel
45	chr12:29300600-29301000	Enhancers	NHEK	skin
46	chr12:29300600-29301200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr12:29300600-29301200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:29300600-29301600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr12:29300600-29301600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:29300600-29301800	Flanking Active TSS	Primary hematopoietic stem cells	blood

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