Variant report

Variant	rs1874911
Chromosome Location	chr12:49741538-49741539
allele	C/G
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	CTCF	chr12:49741480-49741630	HRE	kidney:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
2	CTCF	chr12:49741360-49741737	T-47D	breast:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
3	CTCF	chr12:49741429-49741705	GM13977	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
4	CTCF	chr12:49741500-49741650	HMEC	breast:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
5	CTCF	chr12:49741404-49741721	Lung_OC	lung:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
6	PAX5	chr12:49740952-49741728	GM12878	blood:	n/a	chr12:49741295-49741313 chr12:49741297-49741314 chr12:49741296-49741315
7	BHLHE40	chr12:49741421-49741924	HepG2	liver:	n/a	n/a
8	MAX	chr12:49740402-49742031	MCF-7	breast:	n/a	n/a
9	GTF2F1	chr12:49741491-49741583	K562	blood:	n/a	n/a
10	RAD21	chr12:49741447-49741620	GM12878	blood:	n/a	chr12:49741554-49741566 chr12:49741552-49741571 chr12:49741556-49741570
11	CTCF	chr12:49741196-49741705	GM19239	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
12	CTCF	chr12:49741440-49741590	BJ	skin:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
13	YY1	chr12:49741340-49741732	GM12892	blood:	n/a	chr12:49741710-49741721 chr12:49741662-49741676 chr12:49741565-49741577 chr12:49741552-49741566
14	GTF2F1	chr12:49740854-49741837	Hela-S3	cervix:	n/a	n/a
15	MAX	chr12:49740385-49742027	ECC-1	luminal epithelium:	n/a	n/a
16	MAFK	chr12:49741508-49741826	HepG2	liver:	n/a	chr12:49741627-49741644
17	GTF2F1	chr12:49741467-49741593	H1-hESC	embryonic stem cell:	n/a	n/a
18	EGR1	chr12:49741199-49741709	K562	blood:	n/a	n/a
19	SIN3AK20	chr12:49741499-49741935	HepG2	liver:	n/a	n/a
20	ZNF143	chr12:49741395-49741728	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:49741500-49741650	GM12864	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
22	TCF12	chr12:49740213-49742052	ECC-1	luminal epithelium:	n/a	chr12:49741032-49741042
23	CTCF	chr12:49741350-49741756	K562	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
24	UBTF	chr12:49741449-49741655	K562	blood:	n/a	n/a
25	CTCF	chr12:49741500-49741650	HepG2	liver:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
26	CTCF	chr12:49741500-49741650	HA-sp	spinal cord:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
27	KAP1	chr12:49740630-49741894	HEK293	kidney:	n/a	n/a
28	GABPA	chr12:49741448-49741957	A549	lung:	n/a	n/a
29	SP1	chr12:49741262-49742139	A549	lung:	n/a	chr12:49741868-49741882
30	RAD21	chr12:49741222-49741896	MCF-7	breast:	n/a	chr12:49741554-49741566 chr12:49741552-49741571 chr12:49741556-49741570 chr12:49741706-49741716
31	USF2	chr12:49741330-49741617	H1-hESC	embryonic stem cell:	n/a	n/a
32	SIN3A	chr12:49741471-49741773	H1-hESC	embryonic stem cell:	n/a	chr12:49741591-49741604
33	CTCF	chr12:49741407-49741734	GM10266	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
34	FOSL2	chr12:49740940-49742510	A549	lung:	n/a	chr12:49742311-49742320 chr12:49741845-49741854 chr12:49742312-49742319 chr12:49742311-49742319 chr12:49741670-49741679 chr12:49742307-49742318
35	MAX	chr12:49740435-49742080	A549	lung:	n/a	n/a
36	CTCF	chr12:49741439-49741679	HUVEC	blood vessel:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
37	E2F6	chr12:49740549-49741539	K562	blood:	n/a	chr12:49740739-49740750 chr12:49740613-49740622
38	JUND	chr12:49741377-49741764	K562	blood:	n/a	chr12:49741670-49741679
39	USF1	chr12:49741497-49741734	HepG2	liver:	n/a	n/a
40	CTCF	chr12:49741410-49741713	NHEK	skin:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
41	YY1	chr12:49741412-49741642	GM12878	blood:	n/a	chr12:49741565-49741577 chr12:49741552-49741566
42	CTCF	chr12:49741500-49741650	GM12875	blood:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
43	E2F4	chr12:49741512-49741853	MCF10A-Er-Src	breast:	n/a	chr12:49741671-49741683
44	ZBTB7A	chr12:49738646-49742163	ECC-1	luminal epithelium:	n/a	chr12:49739274-49739281 chr12:49741924-49741935 chr12:49741555-49741564
45	EGR1	chr12:49741176-49741951	HCT-116	colon:	n/a	chr12:49741709-49741719
46	CTCF	chr12:49741429-49741739	Kidney_OC	kidney:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
47	CTCF	chr12:49741500-49741650	HBMEC	blood vessel:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
48	MBD4	chr12:49741344-49741953	HepG2	liver:	n/a	n/a
49	CTCF	chr12:49741360-49741650	A549	lung:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
50	ELF1	chr12:49741427-49741942	HepG2	liver:	n/a	chr12:49741594-49741606 chr12:49741549-49741558

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49741527-49741577	PANC-1	pancreas:	n/a
2	chr12:49741527-49741577	AG09319	gingival:	n/a
3	chr12:49741527-49741577	A549	lung:	n/a
4	chr12:49741527-49741577	HNPCEpiC	eye:	n/a
5	chr12:49741527-49741577	SK-N-MC	brain:	n/a
6	chr12:49741527-49741577	HRCEpiC	kidney:	n/a
7	chr12:49741527-49741577	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:49741527-49741577	K562	blood:	n/a
9	chr12:49741527-49741577	NH-A	brain:	n/a
10	chr12:49741527-49741577	HL-60	blood:	n/a
11	chr12:49741527-49741577	Jurkat	blood:	n/a
12	chr12:49741527-49741577	SK-N-SH_RA	brain:	n/a
13	chr12:49741527-49741577	GM12892	blood:	n/a
14	chr12:49741527-49741577	HMEC	breast:	n/a
15	chr12:49741527-49741577	GM19239	blood:	n/a
16	chr12:49741527-49741577	HUVEC	blood vessel:	n/a
17	chr12:49741527-49741577	SAEC	small airway:	n/a
18	chr12:49741527-49741577	Caco-2	colon:	n/a
19	chr12:49741527-49741577	HRE	kidney:	n/a
20	chr12:49741527-49741577	PFSK-1	brain:	n/a
21	chr12:49741527-49741577	MCF10A-Er-Src	breast:	n/a
22	chr12:49741527-49741577	Hela-S3	cervix:	n/a
23	chr12:49741527-49741577	T-47D	breast:	n/a
24	chr12:49741527-49741577	NHBE	bronchial:	n/a
25	chr12:49741527-49741577	GM06990	blood:	n/a
26	chr12:49741527-49741577	HCM	heart:	n/a
27	chr12:49741527-49741577	NHDF-neo	bronchial:	n/a
28	chr12:49741527-49741577	GM12891	blood:	n/a
29	chr12:49741527-49741577	BJ	skin:	n/a
30	chr12:49741527-49741577	HAEpiC	amniotic membrane:	n/a
31	chr12:49741527-49741577	CMK	blood:	n/a
32	chr12:49741527-49741577	Hepatocyte	liver:	n/a
33	chr12:49741527-49741577	AG04449	skin:	fetal
34	chr12:49741527-49741577	NT2-D1	testis:	n/a
35	chr12:49741527-49741577	HCPEpiC	choroid plexus:	n/a
36	chr12:49741527-49741577	HCT-116	colon:	n/a
37	chr12:49741527-49741577	ECC-1	luminal epithelium:	n/a
38	chr12:49741527-49741577	ProgFib	skin:	n/a
39	chr12:49741527-49741577	HIPEpiC	eye:	n/a
40	chr12:49741527-49741577	SKMC	muscle:	n/a
41	chr12:49741527-49741577	HEK293	kidney:	embryo
42	chr12:49741527-49741577	PrEC	prostate:	n/a
43	chr12:49741527-49741577	AoSMC	blood vessel:	n/a
44	chr12:49741527-49741577	AG10803	skin:	n/a
45	chr12:49741527-49741577	SK-N-SH	brain:	n/a
46	chr12:49741527-49741577	HCF	heart:	n/a
47	chr12:49741527-49741577	HRPEpiC	eye:	n/a
48	chr12:49741527-49741577	NB4	blood:	n/a
49	chr12:49741527-49741577	MCF-7	breast:	n/a
50	chr12:49741527-49741577	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:49688782..49690788-chr12:49741064..49743191,2	MCF-7	breast:
2	chr12:49739423..49741666-chr12:49907974..49910735,2	MCF-7	breast:
3	chr12:49691871..49692482-chr12:49741193..49741985,2	MCF-7	breast:
4	chr12:49656587..49660636-chr12:49733539..49743833,13	K562	blood:
5	chr12:49741030..49742987-chr12:49986875..49988929,2	K562	blood:
6	chr12:49740832..49741606-chr12:49942595..49943430,2	K562	blood:
7	chr12:49739131..49745064-chr12:49758784..49762517,10	MCF-7	breast:
8	chr12:49683076..49686072-chr12:49740867..49742928,2	MCF-7	breast:
9	chr12:49657182..49662198-chr12:49738070..49742868,13	MCF-7	breast:
10	chr12:49740569..49744952-chr12:49759719..49761508,3	K562	blood:
11	chr12:49726361..49727184-chr12:49741012..49741811,2	K562	blood:
12	chr12:49740075..49745225-chr12:49756992..49761732,8	K562	blood:
13	chr12:49740266..49744152-chr12:49960185..49963713,4	MCF-7	breast:
14	chr12:49715312..49722303-chr12:49739075..49744198,13	MCF-7	breast:
15	chr12:49741114..49742103-chr12:50016468..50017223,2	K562	blood:
16	chr12:49725094..49726383-chr12:49741023..49741965,3	MCF-7	breast:
17	chr12:49681907..49682823-chr12:49741104..49742122,6	MCF-7	breast:
18	chr12:49725108..49725946-chr12:49741085..49742047,4	K562	blood:
19	chr12:49740264..49744957-chr12:49759411..49762039,7	MCF-7	breast:
20	chr12:49655321..49661148-chr12:49729487..49743115,26	K562	blood:
21	chr12:49741089..49742059-chr12:49973951..49974946,3	K562	blood:
22	chr12:49656742..49663815-chr12:49736558..49745017,19	MCF-7	breast:
23	chr12:49730689..49731576-chr12:49741266..49741832,2	MCF-7	breast:
24	chr12:49741446..49744429-chr12:50016284..50018933,2	MCF-7	breast:

Variant related genes	Relation type
DNAJC22	TF binding region
DNAJC22	CpG island
ENSG00000167553	Chromatin interaction
ENSG00000187778	Chromatin interaction
ENSG00000186897	Chromatin interaction
ENSG00000110844	Chromatin interaction
ENSG00000135451	Chromatin interaction
ENSG00000199237	Chromatin interaction
ENSG00000258101	Chromatin interaction
ENSG00000123352	Chromatin interaction
ENSG00000258334	Chromatin interaction
ENSG00000258284	Chromatin interaction
ENSG00000135406	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10506284	0.92[EUR][1000 genomes]
rs10506285	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11168981	0.94[ASN][1000 genomes]
rs11831313	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11835071	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12299777	0.87[ASN][1000 genomes]
rs12306866	0.94[ASN][1000 genomes]
rs12310129	0.94[ASN][1000 genomes]
rs12317856	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17123696	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1874909	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1874910	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2270741	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60331259	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60494978	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74089059	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74089062	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74089066	0.92[EUR][1000 genomes]
rs7955245	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	nsv1042122	chr12:49678529-49823168	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1039176	chr12:49678529-49832618	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv899068	chr12:49714103-49924637	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv832405	chr12:49720279-49910862	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers 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	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49738800-49741800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
2	chr12:49738800-49742000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr12:49738800-49742000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
4	chr12:49738800-49742000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
5	chr12:49739000-49741800	Active TSS	Aorta	Aorta
6	chr12:49739000-49742000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:49739000-49742000	Enhancers	Lung	lung
8	chr12:49739000-49742200	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr12:49739200-49742000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
10	chr12:49739200-49742200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
11	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
12	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
14	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
15	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
16	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
19	chr12:49739400-49742000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
21	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
22	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
23	chr12:49739400-49742200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr12:49739600-49742400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
25	chr12:49739800-49741600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:49740000-49741600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:49740000-49741600	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
28	chr12:49740200-49741600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr12:49740200-49741600	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr12:49740200-49741600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:49740200-49741600	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:49740200-49742000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
33	chr12:49740200-49742200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:49740400-49741600	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
35	chr12:49740400-49741600	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:49740400-49741600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 31	rectum
37	chr12:49740400-49741800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
38	chr12:49740400-49742000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
39	chr12:49740400-49742000	Enhancers	Spleen	Spleen
40	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
41	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 2	blood
42	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
43	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Primary T killer memory cells from peripheral blood	blood
44	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
45	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
46	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
47	chr12:49740600-49741600	Flanking Bivalent TSS/Enh	HepG2	liver
48	chr12:49740600-49741800	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 1	blood
49	chr12:49740600-49741800	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
50	chr12:49740600-49741800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain

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