Variant report

Variant	nsv948806
Chromosome Location	chr3:85304744-85463443
allele	n/a
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	CEBPB	chr3:85352519-85352674	A549	lung:	n/a	chr3:85352574-85352585
2	CEBPB	chr3:85423175-85423346	H1-hESC	embryonic stem cell:	n/a	chr3:85423236-85423247
3	CEBPB	chr3:85423114-85423389	IMR90	lung:	n/a	chr3:85423236-85423247
4	CEBPB	chr3:85440642-85440887	H1-hESC	embryonic stem cell:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
5	CEBPB	chr3:85423130-85423398	A549	lung:	n/a	chr3:85423236-85423247
6	CEBPB	chr3:85415054-85415293	HepG2	liver:	n/a	chr3:85415166-85415177
7	CEBPB	chr3:85423124-85423388	HepG2	liver:	n/a	chr3:85423236-85423247
8	CEBPB	chr3:85415076-85415195	H1-hESC	embryonic stem cell:	n/a	chr3:85415166-85415177
9	CEBPB	chr3:85440604-85440910	HepG2	liver:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
10	CEBPB	chr3:85440588-85440884	Hela-S3	cervix:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
11	CEBPB	chr3:85440607-85440855	K562	blood:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
12	CEBPB	chr3:85440573-85440896	A549	lung:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
13	CEBPB	chr3:85320033-85320475	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:85320100-85320366	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:85352460-85352731	HepG2	liver:	n/a	chr3:85352574-85352585
16	CEBPB	chr3:85440575-85440914	IMR90	lung:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
17	CHD2	chr3:85371519-85371543	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr3:85392240-85392390	GM12865	blood:	n/a	n/a
19	CTCF	chr3:85410020-85410170	HA-sp	spinal cord:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
20	CTCF	chr3:85409905-85410322	A549	lung:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
21	CTCF	chr3:85353592-85353817	HUVEC	blood vessel:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
22	CTCF	chr3:85392157-85392332	HepG2	liver:	n/a	n/a
23	CTCF	chr3:85353660-85353810	BJ	skin:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
24	CTCF	chr3:85353940-85354090	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr3:85409970-85410227	K562	blood:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
26	CTCF	chr3:85392201-85392352	GM10248	blood:	n/a	n/a
27	CTCF	chr3:85392140-85392290	GM12873	blood:	n/a	n/a
28	CTCF	chr3:85353720-85353870	A549	lung:	n/a	n/a
29	CTCF	chr3:85410000-85410150	HMF	breast:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
30	CTCF	chr3:85353620-85353770	HRE	kidney:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
31	CTCF	chr3:85392224-85392360	GM13976	blood:	n/a	n/a
32	CTCF	chr3:85409942-85410283	IMR90	lung:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
33	CTCF	chr3:85392157-85392403	LNCaP	prostate:	n/a	n/a
34	CTCF	chr3:85392200-85392350	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr3:85409996-85410228	Pancreas_OC	pancreas:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
36	CTCF	chr3:85409914-85410200	ECC-1	luminal epithelium:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
37	CTCF	chr3:85392200-85392350	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:85392150-85392344	IMR90	lung:	n/a	n/a
39	CTCF	chr3:85410020-85410170	HEK293	kidney:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
40	CTCF	chr3:85392160-85392310	K562	blood:	n/a	n/a
41	CTCF	chr3:85353540-85353690	A549	lung:	n/a	n/a
42	CTCF	chr3:85392220-85392370	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr3:85410013-85410208	Spleen_OC	spleen:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
44	CTCF	chr3:85353620-85353770	HPAF	blood vessel:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
45	CTCF	chr3:85410040-85410190	HA-sp	spinal cord:	n/a	chr3:85410104-85410122 chr3:85410112-85410120 chr3:85410111-85410119 chr3:85410099-85410120 chr3:85410106-85410119
46	CTCF	chr3:85353660-85353810	HRPEpiC	eye:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
47	CTCF	chr3:85353617-85353810	MCF-7	breast:	n/a	chr3:85353708-85353718 chr3:85353704-85353720 chr3:85353706-85353715 chr3:85353705-85353726 chr3:85353703-85353721
48	CTCF	chr3:85392200-85392350	SAEC	small airway:	n/a	n/a
49	CTCF	chr3:85392180-85392330	GM12801	blood:	n/a	n/a
50	CTCF	chr3:85392253-85392346	GM19240	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:85453248..85455514-chr3:85462247..85464334,2	K562	blood:
2	chr3:85453248..85455514-chr3:85462247..85464334,2	K562	blood:
3	chr3:85364029..85366181-chr3:85371658..85373734,2	K562	blood:
4	chr3:85409636..85410536-chr3:85624933..85625875,2	MCF-7	breast:
5	chr3:85454106..85456659-chr3:85459742..85462489,2	K562	blood:
6	chr3:85439579..85441215-chr3:85551442..85553756,2	K562	blood:
7	chr3:84597130..84597691-chr3:85409635..85410581,3	MCF-7	breast:
8	chr3:85353354..85354461-chr3:85391496..85392792,4	MCF-7	breast:
9	chr3:85455981..85458898-chr3:85554544..85556051,2	K562	blood:
10	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
11	chr3:85401815..85404016-chr3:85405205..85407101,2	K562	blood:
12	chr3:85353291..85354669-chr3:85409554..85410988,3	K562	blood:
13	chr3:85353354..85354461-chr3:85391496..85392792,4	MCF-7	breast:
14	chr3:85461933..85464830-chr3:85550203..85551783,2	K562	blood:
15	chr3:85353497..85354172-chr3:85624891..85625399,2	MCF-7	breast:
16	chr3:85454106..85456659-chr3:85459742..85462489,2	K562	blood:
17	chr3:85364029..85366181-chr3:85371658..85373734,2	K562	blood:
18	chr3:85457628..85458566-chr3:130193477..130193997,2	MCF-7	breast:
19	chr3:84992684..84993232-chr3:85391799..85392321,2	MCF-7	breast:
20	chr3:85353413..85354226-chr3:85409666..85410591,2	MCF-7	breast:
21	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
22	chr3:85401815..85404016-chr3:85405205..85407101,2	K562	blood:
23	chr3:85448906..85450732-chr3:85454290..85457141,2	K562	blood:
24	chr3:85353629..85354290-chr3:85624959..85625479,2	K562	blood:
25	chr3:85353254..85353869-chr3:85625261..85626043,2	MCF-7	breast:
26	chr3:85448906..85450732-chr3:85454290..85457141,2	K562	blood:
27	chr3:85353413..85354226-chr3:85409666..85410591,2	MCF-7	breast:
28	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:
29	chr3:85353291..85354669-chr3:85409554..85410988,3	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5688	chr3:85434911-85434932	MIMAT0022479

Variant related genes	Relation type
MIR5688	TF binding region

Extended variants
information (count: 4056 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4056 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12486784	chr3:85304744-85304745	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570432081	chr3:85304771-85304772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145592958	chr3:85304776-85304777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75987623	chr3:85304823-85304824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556281577	chr3:85305064-85305065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568129933	chr3:85305065-85305066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535466760	chr3:85305066-85305067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376448282	chr3:85305069-85305070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142084222	chr3:85305095-85305096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200943922	chr3:85305106-85305107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572343140	chr3:85305111-85305112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545774014	chr3:85305116-85305117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114351558	chr3:85305127-85305128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575817186	chr3:85305128-85305129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543179077	chr3:85305132-85305133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186498617	chr3:85305138-85305139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191340683	chr3:85305161-85305162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183591937	chr3:85305172-85305173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146300869	chr3:85305180-85305181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533729195	chr3:85305229-85305230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551765207	chr3:85305239-85305240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563910685	chr3:85305240-85305241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531146720	chr3:85305242-85305243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186947358	chr3:85305307-85305308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568166193	chr3:85305394-85305395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371452212	chr3:85305401-85305402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139466207	chr3:85305418-85305419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547414321	chr3:85305468-85305469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142807267	chr3:85305470-85305471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539753200	chr3:85305482-85305483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565875644	chr3:85305524-85305525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575902673	chr3:85305525-85305526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536850484	chr3:85305539-85305540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553035914	chr3:85305594-85305595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140007555	chr3:85305605-85305606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541164774	chr3:85305606-85305607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559726668	chr3:85305608-85305609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534546689	chr3:85305632-85305633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545355011	chr3:85305642-85305643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563996550	chr3:85305646-85305647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531185149	chr3:85305647-85305648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576007860	chr3:85305679-85305680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147939148	chr3:85305742-85305743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561461344	chr3:85305803-85305804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529009783	chr3:85305811-85305812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141219568	chr3:85305830-85305831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565734204	chr3:85305842-85305843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375381968	chr3:85305892-85305893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34178549	chr3:85305916-85305917	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550725368	chr3:85305923-85305924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Prostate cancer	21307934	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85288400-85307600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:85303000-85308200	Weak transcription	Brain Germinal Matrix	brain
3	chr3:85303600-85305400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr3:85304200-85305200	Enhancers	Brain Hippocampus Middle	brain
5	chr3:85304200-85305200	Weak transcription	Brain Substantia Nigra	brain
6	chr3:85304200-85307200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:85304400-85307600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr3:85304600-85307200	Weak transcription	Brain Angular Gyrus	brain
9	chr3:85305000-85305400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:85305000-85307200	Weak transcription	Brain Anterior Caudate	brain
11	chr3:85305200-85305600	Enhancers	Brain Substantia Nigra	brain
12	chr3:85305200-85307000	Weak transcription	Brain Hippocampus Middle	brain
13	chr3:85305400-85307200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr3:85305600-85307200	Weak transcription	Brain Substantia Nigra	brain
15	chr3:85307000-85307400	Enhancers	Brain Hippocampus Middle	brain
16	chr3:85307200-85307400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr3:85307200-85307400	Enhancers	Brain Anterior Caudate	brain
18	chr3:85307200-85307600	Enhancers	Brain Angular Gyrus	brain
19	chr3:85307200-85307600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr3:85307200-85307600	Enhancers	Brain Substantia Nigra	brain
21	chr3:85307200-85307600	Enhancers	Fetal Brain Female	brain
22	chr3:85307200-85309000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:85307400-85307600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
24	chr3:85307400-85307600	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr3:85307400-85308400	Active TSS	Brain Anterior Caudate	brain
26	chr3:85307400-85309200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:85307600-85307800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:85307600-85308000	Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr3:85307600-85308200	Active TSS	Brain Cingulate Gyrus	brain
30	chr3:85307600-85308200	Active TSS	Fetal Brain Female	brain
31	chr3:85307600-85308400	Active TSS	Brain Angular Gyrus	brain
32	chr3:85307600-85308400	Active TSS	Brain Hippocampus Middle	brain
33	chr3:85307600-85308400	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr3:85307600-85308400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr3:85307600-85308400	Active TSS	Brain Substantia Nigra	brain
36	chr3:85307600-85309200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:85307800-85308200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:85308000-85308200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr3:85308000-85308400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr3:85308200-85308400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:85308200-85308400	Flanking Active TSS	Brain Cingulate Gyrus	brain
42	chr3:85308200-85308400	Enhancers	Fetal Brain Female	brain
43	chr3:85308200-85309200	Enhancers	Brain Germinal Matrix	brain
44	chr3:85308400-85308600	Weak transcription	Brain Substantia Nigra	brain
45	chr3:85308400-85308800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:85308400-85309600	Weak transcription	Brain Angular Gyrus	brain
47	chr3:85308400-85309800	Weak transcription	Brain Anterior Caudate	brain
48	chr3:85308400-85310000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr3:85308600-85310000	Enhancers	Brain Substantia Nigra	brain
50	chr3:85308800-85309000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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